ライフサイエンスコーパス: diversity in

1 mative EST-SSR markers to assess the genetic diversity in 82 strains of Bailinggu breeding materials.

2 We experimentally manipulated plant diversity in a California serpentine grassland and found

3 We investigated clonal dynamics and diversity in a cohort of 15 ADA-SCID children treated wi

4 NA sequencing can precisely resolve cellular diversity in a high-throughput manner at low cost, but u

5 crobiota to monitor for changes in microbial diversity in a larger cohort of patients.

6 issue by examining the determinants of maize diversity in a local region of high cultural and biologi

7 onnectivity to mediate the rescue of genetic diversity in a natural system.

8 (Prevotella), and Shannon index of microbial diversity in a network analysis.

9 We were able to monitor genetic diversity in a network of populations of the alpine butt

10 We examine how diversity in a population of multisensory neurons may be

11 nogenomic rules that shape immune repertoire diversity in a predictable fashion.

12 ector memory-like profile, it still revealed diversity in a set of natural killer cell-associated rec

13 g species, functional, and phylogenetic beta diversity in a subtropical forest chronosequence in Sout

14 Both markers showed highest genetic diversity in accessions from Ebonyi.

15 Transcriptome diversity in adult neurons is partly mediated by RNA bin

16 However, this view does not explain the diversity in affinity found in IgG variants, such as the

17 Understanding human genetic diversity in Africa is important for interpreting the ev

18 Thus, reduced bacterial diversity in aged mice may contribute to increased P. gi

19 Diversity in aggregate morphology correlates with the di

20 rise to a rich phase diagram displaying high diversity in aggregated states.

21 ver types is purported to decrease arthropod diversity in agroecosystems and is dependent on patterns

22 mentous bacteria, and an increase in species diversity in Ahr(-/-) mice following genotypic segregati

23 D, negligible population structure, and high diversity in an adapted background make the AB-NAM an im

24 d index-variable OTTDL that exploits spatial diversity in an equal length waveguide array.

25 Evaluation of patterns of nucleotide diversity in and near genes shows little evidence of sel

26 y in duration of carriage will also maintain diversity in antibiotic resistance.

27 multiple cell types, accompanied by genetic diversity in antigen receptors.

28 providing a unique perspective into antibody diversity in antigen recognition.

29 raries can be designed that present sequence diversity in architecturally distinct, biologically rele

30 e/cofactor pairs promises to expand cofactor diversity in artificial metalloenzymes.

31 te Triassic and expands its distribution and diversity in Asia.

32 we documented northern populations with low diversity in at least one genetic measure, although most

33 sure that is thought to potentiate antigenic diversity in avian influenza viruses.

34 c noise is a potentially important driver of diversity in bacterial community formation and suggest a

35 The viral diversity in bats is substantial, and viruses with all k

36 ohydrate and protein reveals that stochastic diversity in both CDR3 loops alone almost exclusively ac

37 us expression differences underlie cell fate diversity in both differentiation and disease [2].

38 The T cell compartment must contain diversity in both T cell receptor (TCR) repertoire and c

39 function of normative sex-related phenotypic diversity in brain structure and to identify the pattern

40 mates as a function of normative sex-related diversity in brain structure, as well as neuroanatomical

41 uses, and on overall estimates of seed plant diversity in Brazil and in the neotropics in general, it

42 a significant increase in urinary microbial diversity in burn patients versus controls, which positi

43 plants there appears to have been a loss of diversity in calcium-influx mechanisms at the plasma mem

44 tion as driving force for shaping mitogenome diversity in camels.

45 formation varied in terms of their size and diversity in CD epitopes.

46 ective amplification approaches and the wide diversity in cellular constituents.

47 etable for the Mediterranean diet, while the diversity in chemical composition between the studied sa

48 The results suggest a low level of genetic diversity in Chinese and European populations of C. cili

49 We observe high genetic diversity in circulating strains within and between epid

50 The wild diversity in Coffea (Rubiaceae) genus is large and could

51 d effects on plant community composition and diversity in coming decades.

52 s necessary for explaining trait and species diversity in communities, even in communities with only

53 pective on the role of GABAergic interneuron diversity in cortical development.

54 erent cultivars covering most of the genetic diversity in cultivated apple.

55 key insights on the inclusion of new genetic diversity in cultivated peanut and will inform the devel

56 rials unit survey (46 responses) highlighted diversity in current practice and confirmed support for

57 SCRaMbLE generates genome diversity in designated regions, reveals fitness constra

58 enic centers, is shown to yield considerable diversity in downstream products.

59 of carriage and that mechanisms maintaining diversity in duration of carriage will also maintain div

60 on of pollination services, we highlight the diversity in ecological function mediated by pollinators

61 e genetic variation that explains phenotypic diversity in ecologically relevant characteristics of Ep

62 Maintaining diversity in economic opportunities and enabling turnove

63 cific model system, such an enhanced genetic diversity in environments requiring mutualistic interact

64 rts to delineate the emergence of functional diversity in enzyme superfamilies, provide clues for fun

65 d the distribution of non-genetic phenotypic diversity in Escherichia coli motility, which affects si

66 sively sampled from one university to ensure diversity in ethnic group, age and gender.

67 for generating transcriptomic and proteomic diversity in eukaryotic cells.

68 s, meaning that it is an important driver of diversity in eukaryotic genomes.

69 Haplotype diversity in Europe based on trapped specimens was much

70 s, as well as for the preservation of extant diversity in ex-situ collections.

71 rcial swine populations provides new genetic diversity in exhibition pigs each year locally.

72 eri, we expose nonrandom patterns of genetic diversity in exons that border self-splicing introns.

73 While we documented high genetic and lineage diversity in expanding Patagonian populations, the degre

74 munities and could be a key factor promoting diversity in extreme and/or nutrient-poor environments.

75 th of risky situations in nature that demand diversity in fear behaviors, contemporary neurobiologica

76 ed to recent studies, these findings support diversity in features of kinases that impact on their ac

77 Microbial richness or diversity in fecal samples were not affected.

78 effect of the low FODMAP diet on microbiota diversity in fecal samples.

79 bark and fruit habitats as sources of fungal diversity in ferments.

80 altered by fertilization, with higher alpha diversity in fertilized plots.

81 cessful, understanding genetic and antigenic diversity in field populations is key.

82 Here, we examined bacterial diversity in five ice-covered Antarctic lakes by 16S rRN

83 little is known about species-level genetic diversity in flowering plants outside the eudicots and m

84 To explain diversity in forests, niche theory must show how multipl

85 hich are critical to system miniaturization, diversity in functionality, and non-invasive integration

86 re, we characterized and controlled for this diversity in genome-wide association studies (GWASs) for

87 s to the broader goal of increased ancestral diversity in genomic data resources.

88 ssons and recommendations on how to increase diversity in genomic research studies and the genomic re

89 levels during AIM and a greater evolution of diversity in gp350 nucleotide sequences from AIM to CONV

90 ng-term field study, we show that high plant diversity in grassland systems increases soil aggregate

91 The distribution of genetic diversity in great ape species is likely to have been af

92 and determined its prevalence and molecular diversity in Gyeonggi province, ROK.

93 Amazonia may each contain more tree species diversity in half a square kilometre than do all the tem

94 anisms, we discovered a high transcriptional diversity in HCMV, with many transcripts only slightly d

95 s of fig-living nematodes display remarkable diversity in head morphology depending on their local en

96 c agents are critical modifiers of leukocyte diversity in healing mechanisms that may impair or stimu

97 iscrepancy between the rather low nucleotide diversity in herring and its huge census population size

98 Because of phenotypic diversity in HFpEF, personalized therapeutic strategies

99 High allelic diversity in HLA is argued to be maintained by balancing

100 hich to understand how patterns of taxonomic diversity in hominins may have developed.

101 We found unexpected diversity in hormone-secreting enteroendocrine cells and

102 but the extremely low Y chromosome sequence diversity in horses has prevented the reconstruction of

103 sonal domains are highly variable because of diversity in human ecosystems, evolutionary histories, s

104 sweeps and their combined effects on genomic diversity in humans and other great apes is notoriously

105 nce from rodents, explain the greater T cell diversity in humans and suggest a mechanism for ensuring

106 Increased tag diversity in inactive genes is indicative of a protracte

107 eport remarkable within- and between-species diversity in incubation rhythms.

108 and subsequently tends to lower the genetic diversity in its genome.

109 om bulk lung and pancreas reveals surprising diversity in Kras variant oncogenicity.

110 topics were addressed during the conference: diversity in leadership positions; mentoring; modernizin

111 as implications for achieving stereochemical diversity in library design and diversity-oriented synth

112 are complex enough to mirror the structural diversity in lignin but still of sufficiently low molecu

113 face and explained via the jump model by the diversity in local DNA interfacial topographies and DNA-

114 This diversity in location is paralleled in the many physiolo

115 Finally, we also find that genetic diversity in M. m. castaneus is positively correlated wi

116 inverse association of asthma with bacterial diversity in mattress dust as compared to nasal samples

117 ure was positively associated with bacterial diversity in mattress dust samples as determined by rich

118 ps and the occurrence of variable degrees of diversity in Mesoamerica and the Andes.

119 Despite vast diversity in metabolites and the matching substrate spec

120 Determinants of species diversity in microbial ecosystems remain poorly understo

121 acteria, and Firmicutes as well as a reduced diversity in microbiome.

122 achiropteran bats (megabats) show remarkable diversity in microhabitat occupation and trophic special

123 history and had a profound impact on genetic diversity in modern populations.

124 ghlight the importance of preserving genetic diversity in more isolated high-elevation populations.

125 We found lower levels of genetic diversity in mouflon than in domestic sheep, consistent

126 rns of both inter- and intraspecific genetic diversity in mouse lemur species found in the eastern, w

127 he way to identify the specific role of PMEI diversity in muro.

128 functional differences in the maintenance of diversity in naive and memory pools.

129 omolecules in sequence space, characterizing diversity in natural populations, and experimentally inv

130 the evolution and maintenance of behavioural diversity in natural populations.

131 the evolution and maintenance of behavioural diversity in natural populations.

132 c mechanisms that showcase both the chemical diversity in natural product biosynthesis as well as the

133 mbinant glycoproteins representing the viral diversity in nature.

134 standing of patterns of spatial and temporal diversity in nature.

135 e to underscore the increasing importance of diversity in neurology, to point out some of the specifi

136 ordinated, strategic approaches to enhancing diversity in neurology.

137 h orientation selectivity but also including diversity in neuronal responses, bimodal distributions o

138 order to better prepare trainees and advance diversity in neuroscience, career development must move

139 was strongly related to soil pH, with higher diversity in neutral samples and lower in acidic samples

140 ge expansions, which deeply impacted genetic diversity in newly settled areas and potentially increas

141 ely generate genomic alterations and genetic diversity in normal proliferating cells.

142 hworms are associated with declines in plant diversity in North American forests.

143 We conclude that postvaccine diversity in NVT PNSP between 2009 and 2013 was driven m

144 There was decreased microbial diversity in oesophageal adenocarcinoma tissue compared

145 ray binding and molecular dynamics, reveal a diversity in oligosaccharide affinity and a requirement

146 has also uncovered extensive and unexpected diversity in other MHC genes; an example is MUC22, which

147 ay offers a perspective on the importance of diversity in our educational institutions as well as on

148 cular differentiation, axonal targeting, and diversity, in part by regulating the expression level of

149 gene transfer may contribute to the observed diversity in pathogenic strains.

150 The Cytosponge detected decreased microbial diversity in patients with high-grade dysplasia in compa

151 mparative studies of birds show a remarkable diversity in patterns of change in migratory habits [15-

152 deep sequencing to profile DENV-3 intrahost diversity in peripheral blood mononuclear cell (PBMC) an

153 tions for the role of outer membrane protein diversity in persistent H. pylori infection.

154 The findings suggest that sequence diversity in Pfhrp2 and Pfhrp3 genes in Indian isolates

155 m a large wolf-like progenitor, unparalleled diversity in phenotype and behaviour has developed in do

156 Molecular diversity in phytochemicals of legume extracts was enhan

157 We assessed whether diversity in plant hydraulic traits can explain the obse

158 nt hydraulic traits can explain the observed diversity in plant responses to water stress in seasonal

159 morphogenetic mechanism for generating shape diversity in plants and animals.

160 y ambitious, the aggregate outcomes mask the diversity in progress at the country level.

161 investigated how a single receptor creates a diversity in recognition across myxobacterial population

162 Our data reveal unanticipated diversity in recognition sequences for chaperones; estab

163 sing path analysis, we found that functional diversity in regeneration traits (fire tolerance, fire r

164 to examine microbial community structure and diversity in relation to spatial, temporal and biogeoche

165 neage of 32 extant species, with spectacular diversity in reproductive systems.

166 T treatment resulted in greater TCR sequence diversity in resected prostate tissue in sipuleucel-T-tr

167 Leukocyte diversity in resolving and nonresolving mechanisms of ca

168 screen was performed to explore normal human diversity in responses to rapamycin, a microbial product

169 n cellular components generates cell-to-cell diversity in RNA and protein production dynamics.

170 shotgun sequencing to examine the microbial diversity in samples from the Kalamas River (Northwest G

171 Across plants, leaves exhibit profound diversity in shape.

172 on, and amidation to install broad molecular diversity in short order.

173 hly-variable associations of our scores with diversity in-silico (p < 0.001) and moderate association

174 to ubiquitylated H2A-Lys15 highlighting the diversity in site-specific recognition of ubiquitylated

175 The diversity in size and sequence of orbitides suggests tha

176 , but their importance for shaping microbial diversity in soil remains unclear.

177 Thus, evolutionary diversity in Solanaceae inflorescence complexity is dete

178 rtoires of signaling pathways, and increased diversity in some transcription factor families.

179 More specifically, we consider the diversity in space (nodes or brain regions) over time us

180 the development of >800 new SSDs, increased diversity in SSDs by an average of 34 species, and augme

181 ing with our Q&A series discussing issues of diversity in STEM fields, Genome Biology spoke with thre

182 ing with our Q&A series discussing issues of diversity in STEM fields, Genome Biology spoke with thre

183 Yet the virus shows a remarkable diversity in structural features, often with the same pr

184 ical studies, reveals a key role for cryptic diversity in structuring communities of mutualists.

185 the complexity in NMDAR signaling created by diversity in subunit composition.

186 pandemic risk, owing to an expansion of IAV diversity in swine resulting from long-distance live swi

187 inations, number of mutations and population diversity in terms of its defining parameters.

188 tablish cell-type specificity and functional diversity in terms of motor neuron identities and/or axo

189 We characterize egg-shape diversity in terms of two biologically relevant variable

190 between VS and TF group, and higher baseline diversity in TF patients.

191 fore, salinity levels affected the bacterial diversities in the two low permeability oil blocks remar

192 Higher population genetic diversity in the abundant species is likely due to a com

193 pics in general, it is more likely that tree diversity in the Amazon is closer to the lower estimates

194 e phenotype, yet maintained their structural diversity in the anchorless state.

195 iversity in the E. faecalis group, bacterial diversity in the antibiotic group, especially abundances

196 ct viruses, but the role of this within-host diversity in the antigenic evolution of influenza has be

197 ulations of neurons display an extraordinary diversity in the behaviors they affect and display.

198 , titled "Open Source, Open Door: Increasing Diversity in the Bioinformatics Open Source Community,"

199 o see a great deal of irreducible functional diversity in the brain at multiple spatial scales.

200 Diversity in the degree of such phase dependence could h

201 and temporal hierarchies governing cell-type diversity in the developing human telencephalon, includi

202 Birds display remarkable diversity in the distribution and morphology of scales a

203 ew our current understanding of how neuronal diversity in the dorsal spinal cord is generated and we

204 Bacterial abundance and diversity in the E. faecalis group, bacterial diversity

205 r resolves ambiguity regarding sociality and diversity in the earliest ants.

206 High microbial diversity in the environment has been associated with lo

207 opulation and subsequently promote cell-type diversity in the epidermis.

208 3 cranium augments the previously documented diversity in the European Middle Pleistocene fossil reco

209 mily Chrysopinae includes 97% of the species diversity in the family and it is currently divided into

210 l factor that constrained the alpha and beta diversity in the FE communities.

211 the studied hydroperiods, where high genetic diversity in the first hydroperiod suggested colonisatio

212 linispora reveals extraordinary biosynthetic diversity in the form of 176 distinct biosynthetic gene

213 Modern breeding has dramatically increased diversity in the gene coding regions, though obvious blo

214 g human rhinovirus types includes unexpected diversity in the genes encoding viral proteases (2A(pro)

215 gh levels of both combinatorial and temporal diversity in the granule cell layer.

216 in both blood and gut samples, and increased diversity in the gut during gluten exposure.

217 Microbial diversity in the gut ensures robustness of the microbiot

218 sm of carbohydrate polymers drives microbial diversity in the human gut microbiota.

219 ization of baseline microbial and functional diversity in the human microbiome has enabled studies of

220 population history and migrations-in shaping diversity in the human skull.

221 There is relatively high diversity in the intron region of HsDhn3 compared to the

222 e first time shows the richness of microbial diversity in the Kerala coast and its differences with t

223 Here, we reveal extensive diversity in the kinetic response between 10 and 37 degr

224 is difficult to recapitulate high levels of diversity in the laboratory because of limitations in th

225 natural Tcrb gene rearrangement to generate diversity in the length and composition of CDR3beta.

226 ound an unexpectedly high degree of neuronal diversity in the LTMR-RZ: seven excitatory and four inhi

227 Increased diversity in the magnitude and causes of maternal mortal

228 nt samples, we demonstrate tremendous clonal diversity in the majority of acute myeloid leukemia (AML

229 ors, structural analyses revealed unexpected diversity in the mechanism of activation and molecular s

230 t has become clear that there is significant diversity in the mechanisms employed by individual syste

231 indings call for greater chemical and source diversity in the modelling efforts linking the marine ec

232 d in the formation and establishment of cell diversity in the MOE.

233 howed a strong bottom-up effect on butterfly diversity in the most complex landscapes, but this effec

234 We illustrate how an appreciation of the diversity in the nature of these tasks can lead to impor

235 We found that allelic diversity in the network declined after the demographic

236 illion years ago, giving rise to the current diversity in the New World.

237 There is great diversity in the number of R2R3-MYB genes in different p

238 order to improve our comprehension of viral diversity in the oceans and its relationships with host

239 Strategic Plan to Increase Racial and Ethnic Diversity in the Oncology Workforce is designed to enhan

240 Strategic Plan to Increase Racial and Ethnic Diversity in the Oncology Workforce.

241 Bacterial assemblage diversity in the PA fraction always exceeded the FL frac

242 The extreme low nucleotide diversity in the papaya X-linked region is much greater

243 The extremely low diversity in the papaya X-linked region was probably cau

244 eterogeneity of pathoanatomical subtypes and diversity in the pathogenesis and extent of injury contr

245 Beyond this general framework, considerable diversity in the pattern of network failure was found be

246 Diversity in the physician workforce is essential to pro

247 se opposing aspects of sex require genotypic diversity in the population.

248 ore complex mechanisms generate and maintain diversity in the rare biosphere in this habitat.

249 However, functional sequence diversity in the RBS has not been fully explored.

250 tion of animal hosts lead to reduced genetic diversity in the resulting microbiota and, at low-inocul

251 In contrast to the history of species diversity in the sea and on land [8-10] and the flows of

252 These results suggest that low antigenic diversity in the setting of a unique inflammatory profil

253 GVHD has been associated with low bacterial diversity in the stool microbiota early after transplant

254 es were isoform-specific, indicating a great diversity in the structure of apoE lipoparticles.

255 ween the Jagged and Delta family show a huge diversity in the structures of the loops at the apex of

256 easured GFR and the potential lack of ethnic diversity in the study cohort.

257 Current diversity in the subcontinent is the result of complex e

258 ed by the pervasive inter- and intra-lineage diversity in the targetable mechanisms that underlie KRA

259 spectrometry analyses reveal a huge chemical diversity in the two taxa.

260 of receptive fields in L2/3 is likely due to diversity in the underlying functional circuits.

261 N. meningitidis strains may reflect genetic diversity in the underlying meningococcal population rat

262 remodel microtubules, there is considerable diversity in the underlying molecular mechanisms of micr

263 ottleneck that reduced nonsynonymous genetic diversity in the viral hemagglutinin and nucleoprotein,

264 promotes frequent recombination to increase diversity in the viral population.

265 changes in bird functional and phylogenetic diversity in the wake of extinctions and introductions a

266 The composition, abundance and diversity in the WM and SDM were relatively stable over

267 cestry populations have the greatest genomic diversity in the world, and this diversity has important

268 e mapped compositional variation (i.e., beta-diversity) in the gut microbiotas of 136 pairs of wild m

269 a wide range of behaviors, which reflect the diversity in their chemical compositions, and many are e

270 Although the complexes display considerable diversity in their composition and architecture, many ba

271 nt stimulus, Re neurons display considerable diversity in their firing patterns.

272 is of the tip cell lamellipodia revealed the diversity in their interaction behavior under certain co

273 they achieved considerable ecomorphological diversity in their own right.

274 fish species exhibited substantial response diversity in their sensitivity to land development; for

275 Functional diversity in thermal affinity within the piscivore guild

276 The processes that led to functional diversity in these lineages, which may contribute to a h

277 arvation, may be a key factor underlying the diversity in these rhythms.

278 ly results in very similar levels of neutral diversity in these very different insects.

279 dine inhibition of BM2 and reveal structural diversities in this family of viral proton channels.

280 he species phylogeny and patterns of genetic diversity in this group.

281 ses and for evolutionary analysis of genetic diversity in this region.

282 ent of MYC expression, suggesting biological diversity in this subset of disease.

283 suggest refined lessons for managing genetic diversity in today's warming world.

284 educing productivity [7-10] and life-history diversity in traits such as the spatial and temporal pat

285 ce and facility gender equality, equity, and diversity in transplantation.

286 pecific T cells and an expansion of sequence diversity in treated mice.

287 ework for explaining the maintenance of tree diversity in tropical forests.

288 el might fuel alpha- and beta- components of diversity in tropical sky islands.

289 powerful tool for resolving transcriptional diversity in tumors, but is limited by throughput, cost

290 This diversity, in turn, contributes to a widening gap or dif

291 wildflower plantings on remnant native plant diversity in urban and peri-urban settings has not recei

292 This diversity in valence representations may support the rol

293 analyses revealed extensive loss of genetic diversity in VNBI, suggestive of a history of population

294 g behaviour, as a leading factor driving the diversity in vomeronasal-lingual morphology among lacert

295 In this article, we examine MHC class I diversity in wild mallard ducks, the natural host and re

296 approach to investigate blood-borne pathogen diversity in wild vertebrates and could be used as an ea

297 Understanding patterns of viral diversity in wildlife and determinants of successful cro

298 tion in both phenotypes, despite low genetic diversity in Wolbachia and mtDNA.

299 Here, we have identified geographical diversity in wSuz in D. suzukii populations from differe

300 ic roles of most TALEs, and the overall TALE diversity in Xanthomonas spp. is not known.